Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
Ethics in Clinical Research
Compensating Research Participants FAQ
Blog Posts
What Are Clinical Trials and How Do They Benefit Participants?
Blog Posts
Clinical Endpoints
Recent Innovations and their Regulatory Implications for Multiple Sclerosis Trials Addressed in a Special Issue of the Journal of Clinical Neurophysiology by VeraSci Experts
Blog Posts
Ethics in Clinical Research
What questions can be asked when screening patients prior to them signing consent?
Blog Posts
Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
Blog Posts
FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
Clinical Endpoints
The Parkinson’s Foundation and the Parkinson’s Study Group Provide Recommendations on Overcoming Challenges in Telehealth for Clinical Research Studies
Blog Posts
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
Clinical Endpoints